A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080806



Internal ID21436986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110677345..110677567hg38UCSC Ensembl
chr13:111329692..111329914hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598465
Supporting Variants
SamplesHG00731
Known GenesCARS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080806
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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